A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981387



Internal ID54961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40011666..40014658hg38UCSC Ensembl
chr6:39979405..39982397hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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